Dosage & Administration
Apply to affected areas not more than 1-3 times daily.
Camphor
FDA Label NDC 80465-015
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Eros Global Corp for the product Camphor (NDC 80465-015). This document serves as the official prescribing information, containing essential scientific data and clinical materials required for healthcare providers and patients.
This specific version of the label includes detailed information regarding dosage & administration, warnings, inactive ingredient, indications & usage, otc - keep out of reach of children, otc - purpose, otc - active ingredient, package label.principal display panel, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Warnings
For external use only.
Avoid contact with eyes.
If you are breastfeeding, consult a health care practitioner prior to use.
Inactive Ingredient
Aqua, Caprylic/Capric Triglyceride, Paraffinum Liquidum, Glyceryl Stearate, PEG-100 Stearate, Dimethicone, Petrolatum, Cetyl Alcohol, Propylene Glycol, Diazolidinyl Urea, Methylparaben, Propylparaben, Triethanolamine, Thymus Vulgaris (Thyme) Oil, Stearyl Alcohol, Parfum, Carbomer, Canola Oil, Rosmarinus Officinalis (Rosemary) Oil, Citral, D-Limonene, Geraniol, Linalool.
Indications & Usage
Helps relieve respiratory discomfort, cough, and congestion.
Otc - Keep Out Of Reach Of Children
Keep out of reach of the children.
Otc - Purpose
External Analgesic
Otc - Active Ingredient
Camphor……………………………………..………………….……... 0.15%
* Please review the disclaimer below.
